Medical education — clinical reasoning skills (emergency medicine) Other
Conditions
Interventions
Participants are randomised 1:1 to one of two parallel groups (30 participants per group), using a simple, unrestricted allocation sequence with no stratification or blocking. The sequence is generate
investigators provide no pedagogical input beyond ensuring protocol adherence. In the control group, participants solve the same cases without any digital assistance.
Immediately after the session (
Sponsors
Cadi Ayyad University
Eligibility
Sex/Gender
All
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: 1. Fifth- or sixth-year medical students 2. Undertaking a clinical rotation in emergency medicine or intensive care 3. Provided written, free and informed consent
Exclusion criteria
Exclusion criteria: 1. Refusal to participate 2. Prior participation in the pilot study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Documented clinical reasoning quality measured using the total Revised-IDEA (R-IDEA) score, scored independently by two blinded raters at T0 (immediately after the intervention session) and T1 (1 month after the intervention session, under unassisted conditions);Retention of documented clinical reasoning measured using the total R-IDEA score, rated by the same two blinded assessors at T0 (immediately after the intervention session) and T1 (1 month after the intervention session, under unassisted conditions) | — |
Secondary
| Measure | Time frame |
|---|---|
| Participants' perceived usefulness, decisional confidence and motivation regarding ChatGPT use (intervention group only) measured using 13-item, 5-point Likert-type satisfaction questionnaire at T0 (immediately after the intervention session) | — |
Countries
Morocco
Contacts
Public ContactHayate Errifaiy
Outcome results
None listed